Class Class II
Remanufactured EndoWrist ProGrasp Forceps (420093) (K241872)
Description
Remanufactured EndoWrist ProGrasp Forceps (420093) by Rebotix, an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241872
Clearance Date2024-11-07
Clearance TypeTraditional
Product CodeQSM
Regulation Number876.1500
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241872
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Remanufactured EndoWrist ProGrasp Forceps (420093) (K241872) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K203632 | da Vinci S/Si (IS2000/IS3000) 5mm and 8mm Reusable Instrume... | Intuitive Surgical, Inc. | 2021 |
| K081137 | INTUITIVE SURGICAL DA VINCI SI SURGICAL SYSTEM: MODEL IS3000 | Intuitive Surgical, Inc. | 2009 |
| K050369 | INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODEL IS2000 | Intuitive Surgical, Inc. | 2005 |
Trace the full predicate network for K241872
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.